Lumbar PunctureNCT07074925
Video-Assisted Informed Consent for Neonatal Lumbar Puncture
A study testing Video assisted informed consent and Standard consent in people with Lumbar Puncture and Pediatrics, run by University of Texas at Austin at 1 site in United States.
Trial summary
The purpose of this study is to explore the effectiveness of video-assisted neonatal lumbar puncture consent processes against a conventional consent discussion to inform parents about pediatric lumbar puncture in the pediatric ED. Read more about this study
- Who is it for?
- Ages 0 to 7 months
- Conditions the study is for
- Lumbar Puncture, Pediatrics, Emergency Department Patient
- What is being tested?
- Video assisted informed consent and Standard consent
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 100 participants
- Where
- 1 siteUnited States
- Study dates
- 1 Oct 2023to 15 Nov 2025
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 0 to 7 months
- All sexes
- No healthy volunteers
- Child
Who may be able to join
- Children, age 0-7 months old who are recommended for lumbar puncture procedure during an ED visit.
- Caregiver fluent in English or Spanish
Who cannot join
- Previous enrollment in the study, i.e., the patient has been previously part of the current LP study. This will be confirmed by the study coordinator, PI, or co-I.
- Parent/guardian unwilling to complete surveys
Trial locations and contacts
1 site in 1 country.
About this study
The purpose of this study is to explore the effectiveness of video-assisted neonatal lumbar puncture consent processes against a conventional consent discussion to inform parents about pediatric lumbar puncture in the pediatric ED. We hypothesize that having a visual aid in addition to the verbal information presented in the consent process will lead to increased parent comprehension, decision-making, and satisfaction with the consent process. Furthermore, the findings from this study may have broader implications for improving the informed consent process for other medical procedures and interventions in pediatric settings.
Read the detailed description
A neonatal lumbar puncture (LP), also known as a spinal tap, is a critical diagnostic procedure for detecting and managing serious infections such as meningitis in newborns. Ensuring that parents and caregivers fully understand the procedure, its risks, and its benefits is an essential aspect of the informed consent process. Traditionally, healthcare providers have relied on verbal and written methods to communicate this information to parents, aiming to facilitate comprehension and obtain consent for the procedure. However, there is growing evidence that these traditional methods may not always be sufficient in providing parents with a comprehensive understanding of the procedure, which could potentially impact the decision-making process and overall satisfaction with the care provided. After conventional consent discussions, parents are still often not aware of what the procedure will entail, the risks, how long the procedure will take, and what outcomes to expect. Language barriers can also contribute to misunderstandings during the consent process, even with the assistance of translation services.
Despite the importance of obtaining informed consent for neonatal LPs, there is a notable lack of research on the effectiveness of alternative methods for communicating this information, such as video-assisted consent. Video-based interventions have been shown to improve patient understanding and satisfaction in other medical contexts and may provide a more engaging and easily accessible means of conveying complex information related to the neonatal lumbar puncture procedure. Integrating video-assisted consent into the process could potentially enhance parent comprehension, decision-making, and satisfaction with the consent process.
The purpose of this study is to explore the effectiveness of video-assisted neonatal lumbar puncture consent processes against a conventional consent discussion to inform parents about pediatric lumbar puncture in the pediatric ED. We hypothesize that having a visual aid in addition to the verbal information presented in the consent process will lead to increased parent comprehension, decision-making, and satisfaction with the consent process. Furthermore, the findings from this study may have broader implications for improving the informed consent process for other medical procedures and interventions in pediatric settings.
A video-assisted informed consent intervention will be implemented in the Dell Children's Medical Center (DCMC) Emergency Department (ED). Parents whose children are recommended for LP will be randomly selected to receive either standard informed consent procedures or video-assisted informed consent. We plan to enroll 100 participants. The intervention group (n=50) will receive procedure information via a video and the control group (n=50) will receive standard procedure explanation. The 2-minute video (available in English or Spanish) will use animation to explain the neonatal LP procedure, benefits, and risks.
All participants will complete brief knowledge surveys after the intervention and will be asked to provide feedback on their satisfaction with the informed consent process. Pediatric emergency medicine physicians at Dell Children's collaborated to create the knowledge surveys using the Delphi method. The primary outcome to be assessed is the efficacy of the video intervention on parents' comprehension compared to the conventional discussion. Secondary outcomes will focus on parental satisfaction with the informed consent process and the rate of consent refusal.
- Being tested
- Video assisted informed consent, Standard consent
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Video assisted informed consentOther
The 2-minute video (available in English or Spanish) will use animation to explain the neonatal LP procedure, benefits, and risks.
Standard consentOther
The standard consent group will receive usual procedure description and consent.
| Study group | Role | What they receive |
|---|---|---|
| Video assisted consent | Experimental | The intervention group (n=50) will receive procedure information via a video explanation. The 2-minute video (available in English or Spanish) will use animation to explain the neonatal LP procedure, benefits, and risks. Receives: Other: Video assisted informed consent |
| Standard consent | Active comparator | The control group (n=50) will receive standard procedure explanation. Receives: Other: Standard consent |
What is being measured
The primary outcome is the main question the study is designed to answer.
Comprehension efficacy
Efficacy of the video intervention on parents' comprehension compared to the conventional consent discussion of the lumbar puncture procedure. Using the Delphi method, a knowledge survey was designed. The survey consists of 10 questions about the lumbar puncture procedure that are discussed in both the standard consent discussion and in the video. Each question has one correct response. The investigators will compare correct responses (individual questions and aggregate scores) between the two groups. The survey will be given to the parents/caregivers immediately after the procedure informed consent process.
Measured: Day 1
Secondary outcomes (1)
Parental satisfaction
Parental satisfaction of the consent process will be obtained using a single question with a Likert scale response option: "How satisfied were you with the consent process for the lumbar puncture procedure? Were you: very satisfied, satisfied, neither satisfied nor dissatisfied, dissatisfied, very dissatisfied." This question is part of a survey that will be given to parents/caregivers immediately after the consent process for the lumbar puncture procedure. Parents/caregivers of both groups will be asked this question and satisfaction ratings of the groups will be compared.
Measured: Day 1
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted20 Jul 2025
- Study start1 Oct 2023
- Primary completion15 Nov 2024
- Study completion15 Nov 2025 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (5)Papers the sponsor has linked to this study.
- Other trials for Lumbar PunctureStudies of the same condition, open and under way.
- More trials run by University of Texas at AustinThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind
- Who is masked
- Participant
- Enrolment
- 100 participants (estimated)
Sponsor and investigators
- Lead sponsor
- University of Texas at Austin
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Lina Palomares, University of Texas at Austin
- Investigators
- Matthew Wilkinson, MD, MPH, Study director, The University of Texas at Austin
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07074925
- Sponsor's protocol ID
- 00004883
- Status last verified
- Jul 2025
- First submitted
- 1 Jul 2025
- Last updated
- 20 Jul 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No: IDP will not be shared to maintain participant confidentiality.
Publications
Spencer SP, Stoner MJ, Kelleher K, Cohen DM. Using a Multimedia Presentation to Enhance Informed Consent in a Pediatric Emergency Department. Pediatr Emerg Care. 2015 Aug;31(8):572-6. doi: 10.1097/PEC.0000000000000513.
PubMed 26221786Richardson V. Patient comprehension of informed consent. J Perioper Pract. 2013 Jan-Feb;23(1-2):26-30. doi: 10.1177/1750458913023001-204.
PubMed 23413533Sherlock A, Brownie S. Patients' recollection and understanding of informed consent: a literature review. ANZ J Surg. 2014 Apr;84(4):207-10. doi: 10.1111/ans.12555.
PubMed 24812707COMMITTEE ON BIOETHICS. Informed Consent in Decision-Making in Pediatric Practice. Pediatrics. 2016 Aug;138(2):e20161484. doi: 10.1542/peds.2016-1484.
PubMed 27456514Leazer RC. Evaluation and Management of Young Febrile Infants: An Overview of the New AAP Guideline. Pediatr Rev. 2023 Mar 1;44(3):127-138. doi: 10.1542/pir.2022-005624.
PubMed 36854834
Study at a glance
From the registry record, last updated by the sponsor on 20 Jul 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Video-Assisted Informed Consent for Neonatal Lumbar Puncture
- ClinicalTrials.gov ID
- NCT07074925
- Acronym / sponsor ID
- 00004883
- Study type
- Interventional
- Recruitment status
- Active, not recruiting
- Enrolment
- 100 participants (estimated)
- Lead sponsor
- University of Texas at AustinUniversity, hospital or other
- Study start
- 1 Oct 2023 (actual)
- Primary completion
- 15 Nov 2024 (actual)
- Study completion
- 15 Nov 2025 (estimated)
- First posted
- 20 Jul 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The purpose of this study is to explore the effectiveness of video-assisted neonatal lumbar puncture consent processes against a conventional consent discussion to inform parents about pediatric lumbar puncture in the pediatric ED. We hypothesize that having a visual aid in addition to the verbal information presented in the consent process will lead to increased parent comprehension, decision-making, and satisfaction with the consent process. Furthermore, the findings from this study may have broader implications for improving the informed consent process for other medical procedures and interventions in pediatric settings.
Detailed description
A neonatal lumbar puncture (LP), also known as a spinal tap, is a critical diagnostic procedure for detecting and managing serious infections such as meningitis in newborns. Ensuring that parents and caregivers fully understand the procedure, its risks, and its benefits is an essential aspect of the informed consent process. Traditionally, healthcare providers have relied on verbal and written methods to communicate this information to parents, aiming to facilitate comprehension and obtain consent for the procedure. However, there is growing evidence that these traditional methods may not always be sufficient in providing parents with a comprehensive understanding of the procedure, which could potentially impact the decision-making process and overall satisfaction with the care provided. After conventional consent discussions, parents are still often not aware of what the procedure will entail, the risks, how long the procedure will take, and what outcomes to expect. Language barriers can also contribute to misunderstandings during the consent process, even with the assistance of translation services.
Despite the importance of obtaining informed consent for neonatal LPs, there is a notable lack of research on the effectiveness of alternative methods for communicating this information, such as video-assisted consent. Video-based interventions have been shown to improve patient understanding and satisfaction in other medical contexts and may provide a more engaging and easily accessible means of conveying complex information related to the neonatal lumbar puncture procedure. Integrating video-assisted consent into the process could potentially enhance parent comprehension, decision-making, and satisfaction with the consent process.
The purpose of this study is to explore the effectiveness of video-assisted neonatal lumbar puncture consent processes against a conventional consent discussion to inform parents about pediatric lumbar puncture in the pediatric ED. We hypothesize that having a visual aid in addition to the verbal information presented in the consent process will lead to increased parent comprehension, decision-making, and satisfaction with the consent process. Furthermore, the findings from this study may have broader implications for improving the informed consent process for other medical procedures and interventions in pediatric settings.
A video-assisted informed consent intervention will be implemented in the Dell Children's Medical Center (DCMC) Emergency Department (ED). Parents whose children are recommended for LP will be randomly selected to receive either standard informed consent procedures or video-assisted informed consent. We plan to enroll 100 participants. The intervention group (n=50) will receive procedure information via a video and the control group (n=50) will receive standard procedure explanation. The 2-minute video (available in English or Spanish) will use animation to explain the neonatal LP procedure, benefits, and risks.
All participants will complete brief knowledge surveys after the intervention and will be asked to provide feedback on their satisfaction with the informed consent process. Pediatric emergency medicine physicians at Dell Children's collaborated to create the knowledge surveys using the Delphi method. The primary outcome to be assessed is the efficacy of the video intervention on parents' comprehension compared to the conventional discussion. Secondary outcomes will focus on parental satisfaction with the informed consent process and the rate of consent refusal.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (participant)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Video assisted consent | Experimental | Other: Video assisted informed consentThe intervention group (n=50) will receive procedure information via a video explanation. The 2-minute video (available in English or Spanish) will use animation to explain the neonatal LP procedure, benefits, and risks. |
| Standard consent | Active comparator | Other: Standard consentThe control group (n=50) will receive standard procedure explanation. |
Who may qualify
- Ages
- 0 to 7 months
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child
Key inclusion criteria (2 listed)
- Children, age 0-7 months old who are recommended for lumbar puncture procedure during an ED visit.
- Caregiver fluent in English or Spanish
Key exclusion criteria (2 listed)
- Previous enrollment in the study, i.e., the patient has been previously part of the current LP study. This will be confirmed by the study coordinator, PI, or co-I.
- Parent/guardian unwilling to complete surveys
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Video assisted informed consentThe 2-minute video (available in English or Spanish) will use animation to explain the neonatal LP procedure, benefits, and risks. | Other | Video assisted consent |
| Standard consentThe standard consent group will receive usual procedure description and consent. | Other | Standard consent |
Primary outcome
Comprehension efficacy
Time frame: Day 1
Efficacy of the video intervention on parents' comprehension compared to the conventional consent discussion of the lumbar puncture procedure. Using the Delphi method, a knowledge survey was designed. The survey consists of 10 questions about the lumbar puncture procedure that are discussed in both the standard consent discussion and in the video. Each question has one correct response. The investigators will compare correct responses (individual questions and aggregate scores) between the two groups. The survey will be given to the parents/caregivers immediately after the procedure informed consent process.
1 secondary outcome
Parental satisfaction
Time frame: Day 1
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 20 Jul 2025.
- Background: PubMed 26221786Spencer SP, Stoner MJ, Kelleher K, Cohen DM. Using a Multimedia Presentation to Enhance Informed Consent in a Pediatric Emergency Department. Pediatr Emerg Care. 2015 Aug;31(8):572-6. doi: 10.1097/PEC.0000000000000513.
- Background: PubMed 23413533Richardson V. Patient comprehension of informed consent. J Perioper Pract. 2013 Jan-Feb;23(1-2):26-30. doi: 10.1177/1750458913023001-204.
- Background: PubMed 24812707Sherlock A, Brownie S. Patients' recollection and understanding of informed consent: a literature review. ANZ J Surg. 2014 Apr;84(4):207-10. doi: 10.1111/ans.12555.
- Background: PubMed 27456514COMMITTEE ON BIOETHICS. Informed Consent in Decision-Making in Pediatric Practice. Pediatrics. 2016 Aug;138(2):e20161484. doi: 10.1542/peds.2016-1484.
- Background: PubMed 36854834Leazer RC. Evaluation and Management of Young Febrile Infants: An Overview of the New AAP Guideline. Pediatr Rev. 2023 Mar 1;44(3):127-138. doi: 10.1542/pir.2022-005624.
- Individual participant dataSharing planned: No. IDP will not be shared to maintain participant confidentiality.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Matthew Wilkinson, MD, MPH study director
The University of Texas at Austin
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Video assisted informed consent and Standard consent in people with Lumbar Puncture and Pediatrics, run by University of Texas at Austin at 1 site in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 2 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: under way, not looking for participants, as of the sponsor's last update on 20 Jul 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Comprehension efficacy (time frame: Day 1). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT07074925, which also lists 5 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 20 Jul 2025.